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<p><b>Новая страница</b></p><div>{{Short description|Taxonomic description}}<br />
{{distinguish|text=congeners – see [[conspecificity]]}}<br />
In [[genetics]], two [[organism]]s that differ in only one [[Locus (genetics)|locus]] and a linked segment of chromosome are defined as '''congenic'''.<ref>{{cite web | url = http://www.biology-online.org/dictionary/Congenic | title = Congenic - definition from Biology-Online.org | work = Biology-Online.org dictionary | publisher = Biology-Online.org | access-date = 25 August 2017 | archive-date = 8 August 2017 | archive-url = https://web.archive.org/web/20170808235649/http://www.biology-online.org/dictionary/Congenic | url-status = dead }}</ref> Similarly, organisms that are [[Coisogenic strain|coisogenic]] differ in one locus only and not in the surrounding chromosome. Unlike congenic organisms, coisogenic organisms cannot be bred and only occur through spontaneous or targeted mutation at the locus.<br />
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==Generating congenic strains==<br />
Congenic [[Strain (biology)|strains]] are generated in the laboratory by mating two inbred strains (usually rats or mice), and [[Backcrossing|back-crossing]] the descendants 5–10 generations with one of the original strains, known as the ''recipient'' strain. Typically, selection for either phenotype or genotype is performed prior to each back-cross generation. In this manner, either an interesting phenotype, or a defined chromosomal region assayed by genotype, is passed from the ''donor'' strain onto an otherwise uniform ''recipient'' background. Congenic mice or rats can then be compared to the pure recipient strain to determine whether they are phenotypically different if selection was for a genotypic region, or to identify the critical genetic locus, if selection was for a phenotype.<br />
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Speed congenics can be produced in as little as five back-cross generations,<ref>{{cite journal |author=Markel P |title=Theoretical and empirical issues for marker-assisted breeding of congenic mouse strains |journal=Nat. Genet. |volume=17 |issue=3 |pages=280–284 |date=November 1997 |pmid=9354790 |doi=10.1038/ng1197-280 |name-list-style=vanc|author2=Shu P |author3=Ebeling C |display-authors=3 |last4=Carlson |first4=George A. |last5=Nagle |first5=Deborah L. |last6=Smutko |first6=John S. |last7=Moore |first7=Karen J.|s2cid=25212164 }}</ref> through the selection at each generation of offspring that not only retain the desired chromosomal fragment, but also 'lose' the maximum amount of background genetic information from the donor strain. This is also known as ''marker-assisted'' congenics, due to the use of genetic markers, typically [[Microsatellite (genetics)|microsatellite]] markers, but now, more commonly, [[single nucleotide polymorphism]] markers (SNPs). The process can be further aided by the [[superovulation]] of females, to produce many more eggs.<br />
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==See also==<br />
* [[Gene knockout]]<br />
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==Notes and references==<br />
{{reflist}}<br />
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==Further reading==<br />
Congenic strains are discussed in detail in Lee Silver's online book ''Mouse Genetics: Concepts and Applications'':<br />
* {{cite web | url = http://www.informatics.jax.org/silver/frames/frame3-3.shtml | title = Mouse Genetics: Concepts and Applications | work = Lee Silver | access-date = 2007-10-18}}[http://www.informatics.jax.org/silver/frames/frame3-3.shtml]<br />
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[[Category:Genetics]]<br />
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